<i>KCNG1</i>-Related Syndromic Form of Congenital Neuromuscular Channelopathy in a Crossbred Calf
Inherited channelopathies are a clinically and heritably heterogeneous group of disorders that result from ion channel dysfunction. The aim of this study was to characterize the clinicopathologic features of a Belgian Blue x Holstein crossbred calf with paradoxical myotonia congenita, craniofacial d...
Main Authors: | Joana G. P. Jacinto, Irene M. Häfliger, Eylem Emek Akyürek, Roberta Sacchetto, Cinzia Benazzi, Arcangelo Gentile, Cord Drögemüller |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-11-01
|
Series: | Genes |
Subjects: | |
Online Access: | https://www.mdpi.com/2073-4425/12/11/1792 |
Similar Items
-
Muscle channelopathies and electrophysiological approach
by: Cherian Ajith, et al.
Published: (2008-01-01) -
Case report: Coexistence of myotonia congenita and Brugada syndrome in one family
by: Ann Cordenier, et al.
Published: (2022-09-01) -
Case report: Sodium and chloride muscle channelopathy coexistence: A complicated phenotype and a challenging diagnosis
by: Serena Pagliarani, et al.
Published: (2022-08-01) -
An Up-to-Date Overview of the Complexity of Genotype-Phenotype Relationships in Myotonic Channelopathies
by: Fernando Morales, et al.
Published: (2020-01-01) -
Autosomal recessive myotonia congenita, a muscle channelopathy, presenting in Nigerian siblings: A report
by: Ikenna O Onwuekwe, et al.
Published: (2008-01-01)